Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_assertion description "[Rubinstein-Taybi syndrome (RSTS) can be caused by heterozygous mutations or deletions involving CREBBP or, less commonly, EP300.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_assertion evidence source_evidence_literature NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_assertion SIO_000772 25712426 NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_assertion wasDerivedFrom befree-2016 NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_assertion wasGeneratedBy ECO_0000203 NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266122.RA19jpnOFgd7r-DL1y4Mkaf61l_wkg82OIXku3ERQOSlI130_provenance.